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rs878853376

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853376(A;T)
Make rs878853376(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77189468
GeneMYO7A
is asnp
is mentioned by
dbSNPrs878853376
ebirs878853376
HLIrs878853376
Exacrs878853376
Varsomers878853376
Maprs878853376
PheGenIrs878853376
hapmaprs878853376
1000 genomesrs878853376
hgdprs878853376
ensemblrs878853376
gopubmedrs878853376
geneviewrs878853376
scholarrs878853376
googlers878853376
pharmgkbrs878853376
gwascentralrs878853376
openSNPrs878853376
23andMers878853376
23andMe allrs878853376
SNP Nexus

SNPshotrs878853376
SNPdbers878853376
MSV3drs878853376
GWAS Ctlgrs878853376
Max Magnitude0
ClinVar
Risk rs878853376(T;T)
Alt rs878853376(T;T)
Reference rs878853376(A;A)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene MYO7A
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000011.9:g.76900513A>T
CLNSRC
CLNACC RCV000225423.1,